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==Initial Assessment==
1. Is the patient anemic?
*Hgb < 115 in females, < 125 in males
 
2. Is this anemia acute or chronic?
 
3. Is this dilutional anemia? (hematocrit)
 
4. What is the size of the RBC? (MCV)
 
5. Is body appropriately responding? (reticulocyte count)
 
6. What does the peripheral blood smear show?
 
{| border="1" cellpadding="2" cellspacing="0"
|-
|'''MCV < 80'''
'''(hypochromic)'''
|'''normocytic (normochromic)'''
'''low reticulocytes'''
|'''normocytic'''
'''high reticulocytes'''
|'''MCV > 100'''
|-
|Fe deficiency
 
Anemia of chronic disease (ACD)
|chronic liver disease
 
thalassemia trait
 
liver disease
 
megaloblastic
 
marrow failure (pancytopenia)
 
myelodysplasia
 
leukemia
 
alcohol
 
myeloma
 
hypothyroidism
 
mets
 
infection
 
|blood loss
 
hemolysis
 
|lead overload
 
renal failure (uremia)
 
B12 lack
 
sideroblastic
 
endocrine (thyroid)
 
folate lack
 
ACD
 
hematinic lack
 
drugs
|}
 
==Microcytic==
 
*Fe deficiency - ↓ ferritin, ↑ TIBC
**< 15 confirms, 15 - 25 suggests, 25 - 100 not helpful, > 100 rules out
 
*Anemia of chronic disease (ACD)
**associated with inflammation (RA, infection, carcinoma)
**↓ TIBC (Fe not transferred to developing RBCs)
 
*Thalassemia
**target cells, serum electrophoresis (↑ HbgA2)
 
*Lead poisoning - ↑ serum Pb
 
*Sideroblastic - ↑ in cellular iron uptake
**↑ ferritin, ring sideroblasts
 
 
==Macrocytic==
*megaloblastic anemia - hypersegmented polymorphonucleocytes(PMNs)
*defects in DNA synthesis that lead to hematologic abnormalities
*↓ folate or ↓ vit B12
*drugs: methotrexate, azathioprine (Imuran - immunosuppressant)
 
*'''myelodysplasia'''
**dimorphic smear (micro/macrocytosis)
 
*chronic liver disease
**↑ GGT, target cells
 
 
==Normocytic==
===High reticulocyte===
*Hemolysis
**hypersplenism, drugs, sepsis, autoimmune
**cell morphology (from peripheral smear) is crucial: see below
***↑ LDH, ↑ bilirubin, ↑ serum Hbg, ↓ haptoglobin (Hgb scavenger), + Coombs
 
===Low reticulocyte===
*bone marrow failure
**pancytopenia (↓ WBC, ↓ plt)
**BM aspirate (cell morphology), BM biopsy (structure)
 
==Misc==
===Red cell distributuion width (RDW)===
 
*Normal:
**ACD, thalassemia
 
*Increased
**iron deficiency
**duel deficiency (fe, folate)
**pernicious anemia
**liver disease
**AIHA
 
==Blood smear==
===Shape===
*normal: biconcave
*spherocyte - '''immune hemolytic anemia'''
*schistocytes - MAHA: DIC, vasculitis, prosthetic heart valves, HUS/TTP
*sickle cell - sickle cell disorders
*target cell - liver disease, thalassemia, Fe deficiency
*teardrop cell - myelofibrosis
 
===Distribution===
*'''rouleaux formation''' - aggregates of RBC resembling stacks of coins
*'''paraprotein''' (multiple myeloma)
 
 
===Inclusion===
*nuclei (immature RBC)
**serious medical disease
**severe anemia, leukemia, bone marrow metastases
 
*Heinz bodies (denatured hemoglobin)
**G6PD deficiency
 
*Howell-Jolly bodies
**post-splenectomy, hyposplenism
 
*basophilic stippling (blue granulations of variable size and number, aggregation of ribosomes)
**lead intoxication, thalassemia
 
==Other OSCE modules==
{{OSCE2}}
[[Category:Medicine]][[Category:OSCE]]

Revision as of 15:57, 25 August 2007

Initial Assessment

1. Is the patient anemic?

  • Hgb < 115 in females, < 125 in males

2. Is this anemia acute or chronic?

3. Is this dilutional anemia? (hematocrit)

4. What is the size of the RBC? (MCV)

5. Is body appropriately responding? (reticulocyte count)

6. What does the peripheral blood smear show?

MCV < 80

(hypochromic)

normocytic (normochromic)

low reticulocytes

normocytic

high reticulocytes

MCV > 100
Fe deficiency

Anemia of chronic disease (ACD)

chronic liver disease

thalassemia trait

liver disease

megaloblastic

marrow failure (pancytopenia)

myelodysplasia

leukemia

alcohol

myeloma

hypothyroidism

mets

infection

blood loss

hemolysis

lead overload

renal failure (uremia)

B12 lack

sideroblastic

endocrine (thyroid)

folate lack

ACD

hematinic lack

drugs

Microcytic

  • Fe deficiency - ↓ ferritin, ↑ TIBC
    • < 15 confirms, 15 - 25 suggests, 25 - 100 not helpful, > 100 rules out
  • Anemia of chronic disease (ACD)
    • associated with inflammation (RA, infection, carcinoma)
    • ↓ TIBC (Fe not transferred to developing RBCs)
  • Thalassemia
    • target cells, serum electrophoresis (↑ HbgA2)
  • Lead poisoning - ↑ serum Pb
  • Sideroblastic - ↑ in cellular iron uptake
    • ↑ ferritin, ring sideroblasts


Macrocytic

  • megaloblastic anemia - hypersegmented polymorphonucleocytes(PMNs)
  • defects in DNA synthesis that lead to hematologic abnormalities
  • ↓ folate or ↓ vit B12
  • drugs: methotrexate, azathioprine (Imuran - immunosuppressant)
  • myelodysplasia
    • dimorphic smear (micro/macrocytosis)
  • chronic liver disease
    • ↑ GGT, target cells


Normocytic

High reticulocyte

  • Hemolysis
    • hypersplenism, drugs, sepsis, autoimmune
    • cell morphology (from peripheral smear) is crucial: see below
      • ↑ LDH, ↑ bilirubin, ↑ serum Hbg, ↓ haptoglobin (Hgb scavenger), + Coombs

Low reticulocyte

  • bone marrow failure
    • pancytopenia (↓ WBC, ↓ plt)
    • BM aspirate (cell morphology), BM biopsy (structure)

Misc

Red cell distributuion width (RDW)

  • Normal:
    • ACD, thalassemia
  • Increased
    • iron deficiency
    • duel deficiency (fe, folate)
    • pernicious anemia
    • liver disease
    • AIHA

Blood smear

Shape

  • normal: biconcave
  • spherocyte - immune hemolytic anemia
  • schistocytes - MAHA: DIC, vasculitis, prosthetic heart valves, HUS/TTP
  • sickle cell - sickle cell disorders
  • target cell - liver disease, thalassemia, Fe deficiency
  • teardrop cell - myelofibrosis

Distribution

  • rouleaux formation - aggregates of RBC resembling stacks of coins
  • paraprotein (multiple myeloma)


Inclusion

  • nuclei (immature RBC)
    • serious medical disease
    • severe anemia, leukemia, bone marrow metastases
  • Heinz bodies (denatured hemoglobin)
    • G6PD deficiency
  • Howell-Jolly bodies
    • post-splenectomy, hyposplenism
  • basophilic stippling (blue granulations of variable size and number, aggregation of ribosomes)
    • lead intoxication, thalassemia

Other OSCE modules